Interesting Facts about 2-[Methyl(octadec-9-enoyl)amino]ethanesulfonic Acid
2-[Methyl(octadec-9-enoyl)amino]ethanesulfonic acid, often abbreviated as MES, is a fascinating compound that belongs to the family of amino acids and sulfonic acids. This compound is particularly significant in the field of biochemistry and molecular biology.
Key Features of MES
- Buffering Agent: MES is widely used as a buffering agent in biochemical applications. Its ability to maintain pH stability makes it an essential component in various laboratory settings.
- Biocompatibility: Due to its low toxicity and high biocompatibility, MES is ideal for use in biological experiments, particularly involving proteins and nucleic acids.
- Versatile Applications: This compound finds utility in various fields, including cell culture, chromatography, and as a reagent in enzymatic reactions.
- Temperature Stability: MES exhibits remarkable stability across a range of temperatures, making it a reliable choice for experiments that require precise conditions.
One unique aspect of MES is its ability to effectively protect biomolecules from denaturation, which can occur in harsh experimental environments. This property is particularly valuable in protein purification processes where maintaining the structural integrity of proteins is crucial.
In summary, 2-[Methyl(octadec-9-enoyl)amino]ethanesulfonic acid is not just a simple compound; its multifaceted role in scientific research and industry underscores its importance to the scientific community. As many researchers often say, “the right buffer can make all the difference!”
Solubility of 2-[methyl(octadec-9-enoyl)amino]ethanesulfonic acid
2-[methyl(octadec-9-enoyl)amino]ethanesulfonic acid, often referred to within biochemical contexts, exhibits intriguing solubility characteristics influenced by its structural components. This compound possesses both hydrophilic and hydrophobic elements, contributing to its unique solubility behavior:
In summary, the solubility of 2-[methyl(octadec-9-enoyl)amino]ethanesulfonic acid reflects a fascinating interplay of its molecular architecture, where the polar sulfonate enhances aqueous dissolution, while the non-polar hydrocarbon tail provides a degree of hydrophobicity, allowing for versatile usage across various chemical environments.